Glatiramer Acetate
NDC 47335-991, Glatiramer Acetate, injection, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-991
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206873
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-991 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLATIRAMER ACETATE40 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-991-02 | 47335099102 | 12 BLISTER PACK in 1 CARTON (47335-991-02) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/dfacc3e2-5c91-41de-a377-873276a5cf67NADAC price for package 47335099102
GET /v1/drugs/nadac/47335099102
Use it
Look up 47335-991 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-991 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-991. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.